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Academic Journal

Haptoglobin genotype and outcome after spontaneous intracerebral haemorrhage.

Subjects: Cerebral Hemorrhage/Cerebral Hemorrhage/Cerebral Hemorrhage/*genetics ; Haptoglobins/Haptoglobins/Haptoglobins/*genetics; Aged

  • Source: Journal of neurology, neurosurgery, and psychiatry [J Neurol Neurosurg Psychiatry] 2020 Mar; Vol. 91 (3), pp. 298-304. Date of Electronic Publication: 2020 Jan 10.Publisher: BMJ Publishing Group Country of Publication: England NLM ID: 2985191R Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Haptoglobin genotype and outcome after aneurysmal subarachnoid haemorrhage.

Subjects: Haptoglobins/Haptoglobins/Haptoglobins/*genetics ; Intracranial Aneurysm/Intracranial Aneurysm/Intracranial Aneurysm/*genetics ; Subarachnoid Hemorrhage/Subarachnoid Hemorrhage/Subarachnoid Hemorrhage/*genetics

  • Source: Journal of neurology, neurosurgery, and psychiatry [J Neurol Neurosurg Psychiatry] 2020 Mar; Vol. 91 (3), pp. 305-313. Date of Electronic Publication: 2020 Jan 14.Publisher: BMJ Publishing Group Country of Publication: England NLM ID: 2985191R Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genetic determinants of circulating haptoglobin concentration.

  • Authors : Kazmi N; MRC Integrative Epidemiology Unit (IEU), Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.; Koda Y

Subjects: Alleles*; Haptoglobins/Haptoglobins/Haptoglobins/*analysis; Adolescent

  • Source: Clinica chimica acta; international journal of clinical chemistry [Clin Chim Acta] 2019 Jul; Vol. 494, pp. 138-142. Date of Electronic Publication: 2019 Mar 18.Publisher: Elsevier Country of Publication: Netherlands NLM ID: 1302422 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

A common deletion in the haptoglobin gene associated with blood cholesterol levels among Chinese women.

  • Authors : Zheng NS; Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.; Yale College, Yale University, New Haven, CT, USA.

Subjects: Genetic Association Studies* ; Sequence Deletion*; Asians/Asians/Asians/*genetics

  • Source: Journal of human genetics [J Hum Genet] 2017 Oct; Vol. 62 (10), pp. 911-914. Date of Electronic Publication: 2017 Jun 29.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease.

  • Authors : Bjornsson E; deCODE Genetics/Amgen, Inc., Reykjavik, Iceland.; Faculty of Medicine.

Subjects: Coronary Artery Disease/Coronary Artery Disease/Coronary Artery Disease/*genetics ; Haptoglobins/Haptoglobins/Haptoglobins/*genetics; Adult

  • Source: Human molecular genetics [Hum Mol Genet] 2017 Jun 15; Vol. 26 (12), pp. 2364-2376.Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Haptoglobin (HP) and Haptoglobin-related protein (HPR) copy number variation, natural selection, and trypanosomiasis.

Subjects: DNA Copy Number Variations* ; Selection, Genetic*; Antigens, Neoplasm/Antigens, Neoplasm/Antigens, Neoplasm/*genetics

  • Source: Human genetics [Hum Genet] 2014 Jan; Vol. 133 (1), pp. 69-83. Date of Electronic Publication: 2013 Sep 05.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Molecular and population analysis of natural selection on the human haptoglobin duplication.

  • Authors : Rodriguez S; MRC Centre for Causal Analyses in Translational Epidemiology (CAiTE) Bristol Genetic Epidemiology Laboratories (BGEL), School of Social and Community Medicine, University of Bristol, Oakfield House, Oakfield Grove, Bristol BS8 2BN, United Kingdom. ; Williams DM

Subjects: DNA Copy Number Variations* ; Polymorphism, Single Nucleotide* ; Selection, Genetic*

  • Source: Annals of human genetics [Ann Hum Genet] 2012 Sep; Vol. 76 (5), pp. 352-62. Date of Electronic Publication: 2012 May 21.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0416661 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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